FOXP1

Information FOXP1

Description

Transcriptional repressor. Can act with CTBP1 to synergistically repress transcription but CTPBP1 is not essential (PubMed:11358962, PubMed:14701752). Plays an important role in the specification and differentiation of lung epithelium. Acts cooperatively with FOXP4 to regulate lung secretory epithelial cell fate and regeneration by restricting the goblet cell lineage program; the function may involve regulation of AGR2 (PubMed:11358962, PubMed:22675208). Essential transcriptional regulator of B-cell development (PubMed:16819554). Involved in regulation of cardiac muscle cell proliferation (PubMed:20713518). Involved in the columnar organization of spinal motor neurons. Promotes the formation of the lateral motor neuron column (LMC) and the preganglionic motor column (PGC) and is required for respective appropriate motor axon projections. The segment-appropriate generation of spinal chord motor columns requires cooperation with other Hox proteins (PubMed:18667151, PubMed:18662545). Can regulate PITX3 promoter activity; may promote midbrain identity in embryonic stem cell-derived dopamine neurons by regulating PITX3 (PubMed:20175877). Negatively regulates the differentiation of T follicular helper cells T(FH)s (PubMed:24859450). Involved in maintenance of hair follicle stem cell quiescence; the function probably involves regulation of FGF18 (PubMed:23946441). Represses transcription of various pro-apoptotic genes and cooperates with NF-kappa B-signaling in promoting B-cell expansion by inhibition of caspase-dependent apoptosis. Binds to CSF1R promoter elements and is involved in regulation of monocyte differentiation and macrophage functions; repression of CSF1R in monocytes seems to involve NCOR2 as corepressor. Involved in endothelial cell proliferation, tube formation and migration indicative for a role in angiogenesis; the role in neovascularization seems to implicate suppression of SEMA5B. Can negatively regulate androgen receptor signaling (By similarity). Acts as a transcriptional activator of the FBXL7 promoter; this activity is regulated by AURKA (By similarity). {ECO:0000250|UniProtKB:Q9H334, ECO:0000269|PubMed:14701752, ECO:0000269|PubMed:16819554, ECO:0000269|PubMed:18662545, ECO:0000269|PubMed:18667151, ECO:0000269|PubMed:20175877, ECO:0000269|PubMed:20713518, ECO:0000269|PubMed:22675208, ECO:0000269|PubMed:23946441, ECO:0000269|PubMed:24859450, ECO:0000305|PubMed:20175877, ECO:0000305|PubMed:22675208, ECO:0000305|PubMed:23946441}.; [Isoform 5]: Involved in transcriptional regulation in embryonic stem cells (ESCs). Stimulates expression of transcription factors that are required for pluripotency and decreases expression of differentiation-associated genes. Has distinct DNA-binding specifities as compared to the canonical form and preferentially binds DNA with the sequence 5'-CGATACAA-3' (or closely related sequences) (By similarity). Promotes ESC self-renewal and pluripotency (PubMed:21924763). {ECO:0000250|UniProtKB:Q9H334, ECO:0000269|PubMed:21924763}.(Source UnitProtKB).

Full Name

forkhead box P1

Source UniprotKB

Species

Mus musculus [tax_id: 10090]

Genome

mm10

ReMap Statistics

Datasets
5
Biotypes
2
Peaks
29,551
Non-redundant peaks
20,993

TF Classification

Familly
NA
Sub Familly
NA

Source JASPAR

External IDs

NCBI Gene
108655
Official Gene Name
Foxp1
JASPAR
MGI
MGI:1914004
Ensembl
ENSMUSG00000030067
UniProt
P58462
Genevisible
P58462
RefSeq
Aliases
3110052D19Rik; 4932443N09Rik
All peaks FOXP1
Download BED file
Non redundant peaks FOXP1
Download BED file
SEQUENCES FOXP1
Download FASTA file
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Datasets Table for FOXP1

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
FOXP1 lymphocyte Treg_Foxp1-deficient GEO Mus musculus GSE121279 184
FOXP1 lymphocyte Treg GEO Mus musculus GSE121279 10,874
FOXP1 lymphocyte Tconv GEO Mus musculus GSE121279 9,304
FOXP1 mammary-epithelium luminal GEO Mus musculus GSE118618 451
FOXP1 mammary-epithelium basal GEO Mus musculus GSE118618 8,738
Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks